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Hydrochloric Acid → HCID 131730401, 화합물

HRID 1963404
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HRID 1963404 반응식
[C:1]([C:5]1[S:9][C:8]([CH:10]2[CH2:15][CH:14](C(O)=O)[CH2:13][CH2:12][N:11]2[C:19]([O:21][CH3:22])=[O:20])=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].N1(C(N2C=CN=C2)=O)C=CN=C1.[CH2:35]([O:37][C:38](=[O:43])[CH2:39][C:40](O)=[O:41])[CH3:36].[K].[Cl-].[Mg+2].[Cl-].Cl>C1COCC1>[C:1]([C:5]1[S:9][C:8]([C@H:10]2[CH2:15][C@@H:14]([C:40](=[O:41])[CH2:39][C:38]([O:37][CH2:35][CH3:36])=[O:43])[CH2:13][CH2:12][N:11]2[C:19]([O:21][CH3:22])=[O:20])=[CH:7][CH:6]=1)([CH3:2])([CH3:4])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 6

HCID 313Hydrochloric AcidHCID 682631,1'-CarbonyldiimidazoleHCID 70615Monoethyl malonateHCID 5360315Magnesium ChlorideHCID 5462222PotassiumHCID 66731515HCID 66731515, 화합물2회

생성물 1

HCID 131730401
HCID 131730401, 화합물
수율 70.4%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

2-(5-tert-Butylthiophen-2-yl)-1-(methoxycarbonyl)piperidine-4-carboxylic acid (1.125 g, 3.46 mmol) (reference compound 18) was dissolved in THF (30 mL) and di(1H-imidazol-1-yl)methanone (0.911 g, 5.62 mmol) added. The suspension was stirred at room temperature under nitrogen for 6 h (flask 1). In a separate flask 3-ethoxy-3-oxopropanoic acid, potassium salt (1.509 g, 8.82 mmol) and magnesium chloride (0.84 g, 8.82 mmol) were suspended in THF (30 mL) and stirred with an oversized stirring bar at 50° C. under nitrogen for 20 h (flask 2). The white suspension in flask 2 was then added to flask 1. The thick white suspension was stirred at room temperature for 18 h. The reaction mixture was acidified by addition of 3 M HCl to pH 1. The solvent was evaporated in vacuo. MTBE (250 mL) and water were added, shaken and the phases separated. The organic phase was washed with water (200 mL), satd NaHCO3 (200 mL), brine (200 mL), dried with a phase separator and evaporated in vacuo. The residue was purified by automated flash chromatography on a Biotage® KP-SIL 100 g column. A gradient from 10% EtOAc in heptane over 2 CV followed by 10% to 40% of EtOAc in heptane over 9 CV was used as mobile phase. Cis-methyl 2-(5-tert-butylthiophen-2-yl)-4-(3-ethoxy-3-oxopropanoyl)piperidine-1-carboxylate (0.963 g, 70.4%) was isolated. Cis-isomer: MS m/z 396 (M+H)+

후처리

  1. stirringstirred with an oversized stirring bar at 50° C. under nitrogen for 20 h (flask 2)
  2. additionThe white suspension in flask 2 was then added to flask 1
  3. stirringThe thick white suspension was stirred at room temperature for 18 h
  4. customThe solvent was evaporated in vacuo
  5. additionMTBE (250 mL) and water were added
  6. stirringshaken
  7. customthe phases separated
  8. washThe organic phase was washed with water (200 mL), satd NaHCO3 (200 mL), brine (200 mL)
  9. customdried with a phase separator
  10. customevaporated in vacuo
  11. customThe residue was purified by automated flash chromatography on a Biotage® KP-SIL 100 g column

출처 및 근거

ORD 기록
ord-668e65564bc144be8ba49a14ed91a0f9
출처 데이터셋
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08415378B2

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